chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95257185452571857CTT---6GENIChomozygous53112522
95257215752572158GA25GENIChomozygous51956689
95257223752572238TC25GENIChomozygous51956692
95257285452572855GT37GENIChomozygous51956695
95257290352572904AG43GENIChomozygous51956698
95257291752572918GT42GENIChomozygous51956701
95257312052573121AG32GENIChomozygous51956704
95257317852573179TC37GENIChomozygous51956707
95257320852573209AT34GENIChomozygous51956710
95257323452573235CA33GENIChomozygous51956713
95257334052573341TA24GENIChomozygous51956716
95257362752573628AG34GENIChomozygous51956719
95257373052573733TAG---31GENIChomozygous51956722
95257378952573790TA14GENIChomozygous51956725
95257419252574193AG26GENIChomozygous51956728
95257447552574476GA22GENIChomozygous51956731
95257448952574490CT26GENIChomozygous51956734
95257469652574697TC26GENIChomozygous51956737
95257473752574738TC22GENIChomozygous51956740
95257512052575121GA26GENIChomozygous51956743
95257545052575451AG17GENIChomozygous51956746
95257567152575672AG17GENIChomozygous51956749
95257626852576269CA21GENICpossibly homozygous51956752
95257628052576281TG23GENIChomozygous51956755
95257632152576322GC26GENIChomozygous51956758
95257651352576514CCT22GENIChomozygous51956761
95257661052576611TC28GENIChomozygous51956765
95257665052576651TA22GENIChomozygous51956768
95257683152576832AG28GENIChomozygous51956771
95257701252577013AT17GENIChomozygous51956774
95257741352577414CT25GENIChomozygous51956777
95257750252577503AT32GENIChomozygous51956780
95257762252577623AG27GENIChomozygous51956783
95257765652577657AG33GENIChomozygous51956786